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MGMT gene promoter methylation correlates with tolerance of temozolomide treatment in melanoma but not with clinical outcome

机译:MGMT基因启动子甲基化与替莫唑胺在黑色素瘤治疗中的耐受性相关,但与临床结果无关

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摘要

BACKGROUND: Despite limited clinical efficacy, treatment with dacarbazine or temozolomide (TMZ) remains the standard therapy for metastatic melanoma. In glioblastoma, promoter methylation of the counteracting DNA repair enzyme O(6)-methylguanine-DNA-methyltransferase (MGMT) correlates with survival of patients exposed to TMZ in combination with radiotherapy. For melanoma, data are limited and controversial.\ud\udMETHODS: Biopsy samples from 122 patients with metastatic melanoma being treated with TMZ in two multicenter studies of the Dermatologic Cooperative Oncology Group were investigated for MGMT promoter methylation. We used the COBRA (combined bisulphite restriction analysis) technique to determine aberrant methylation of CpG islands in small amounts of genomic DNA isolated from paraffin-embedded tissue sections. To detect aberrant methylation, bisulphite-treated DNA was amplified by PCR, enzyme restricted, and visualised by gel electrophoresis.\ud\udRESULTS: Correlation with clinical data from 117 evaluable patients in a best-response evaluation indicated no statistically significant association between MGMT promoter methylation status and response. A methylated MGMT promoter was observed in 34.8% of responders and 23.4% of non-responders (P=0.29). In addition, no survival advantage for patients with a methylated MGMT promoter was detectable (P=0.79). Interestingly, we found a significant correlation between MGMT methylation and tolerance of therapy. Patients with a methylated MGMT promoter had more severe adverse events, requiring more TMZ dose reductions or discontinuations (P=0.007; OR 2.7 (95% CI: 1.32-5.7)). Analysis of MGMT promoter methylation comparing primaries and different metastases over the clinical course revealed no statistical difference (P=0.49).\ud\udCONCLUSIONS: In advanced melanoma MGMT promoter, methylation correlates with tolerance of therapy, but not with clinical outcome.
机译:背景:尽管临床疗效有限,但达卡巴嗪或替莫唑胺(TMZ)的治疗仍然是转移性黑色素瘤的标准疗法。在胶质母细胞瘤中,抵消性DNA修复酶O(6)-甲基鸟嘌呤-DNA-甲基转移酶(MGMT)的启动子甲基化与暴露于TMZ的放射治疗患者的生存相关。对于黑色素瘤,数据有限且存在争议。\ ud \ ud方法:在皮肤科合作肿瘤学小组的两个多中心研究中,对来自接受TMZ治疗的122例转移性黑色素瘤患者的活检样本进行了MGMT启动子甲基化研究。我们使用了COBRA(亚硫酸氢盐限制结合分析)技术来确定从石蜡包埋的组织切片中分离出的少量基因组DNA中CpG岛的异常甲基化。为了检测异常甲基化,亚硫酸氢盐处理的DNA通过PCR扩增,酶限制并通过凝胶电泳显示。\ ud \ ud结果:与117例可评价患者的临床数据的最佳响应评价表明,MGMT启动子之间无统计学意义的关联甲基化状态和反应。在34.8%的应答者和23.4%的非应答者中观察到甲基化的MGMT启动子(P = 0.29)。另外,没有检测到具有甲基化的MGMT启动子的患者的生存优势(P = 0.79)。有趣的是,我们发现MGMT甲基化与治疗耐受性之间存在显着相关性。具有甲基化MGMT启动子的患者有更严重的不良事件,需要更多的TMZ剂量减少或停药(P = 0.007; OR 2.7(95%CI:1.32-5.7))。分析MGMT启动子甲基化比较临床过程中的原发灶和不同转移没有发现统计学差异(P = 0.49)。\ ud \ ud结论:在晚期黑色素瘤MGMT启动子中,甲基化与治疗耐受性相关,但与临床结果无关。

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